Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1096838860
Device Listing 1096838860
Listing Summary
#
Listing key
1096838860
Premarket submission
K902023
Device
SEAL RITE PROCEDURE KIT(TM)
Applicant
Pulpdent Corp.
Product code
EBC
Decision date
1990-07-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
29912
1215305
1215305
PULPDENT CORPORATION
1
Y
2026-01-01
80 Oakland St Watertown MA US 02472